2 Methyl N Benzylimidazole
quinoline thiophene imidazole thiazole

2-Methyl-N-benzylimidazole

    Specifications

    HS Code

    932891

    Chemical Formula C11H12N2
    Molecular Weight 172.23 g/mol
    Appearance Solid (usually white to off - white powder)
    Melting Point Data depends on purity, typically in a certain range
    Boiling Point Data may vary, specific values based on conditions
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, dichloromethane
    Density Specific value based on experimental determination
    Pka Value Characteristic value related to its acid - base properties
    Flash Point Data relevant for fire - hazard assessment

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    General Information
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    Frequently Asked Questions

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    What are the main uses of 2-Methyl-N-benzylimidazole?
    2-Methyl-N-benzylimidazole has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. Due to its unique structure and active reaction check point, it can construct complex organic molecular structures through various chemical reactions. For example, in the synthesis of heterocyclic compounds, it is often an important starting material, assisting chemists to create novel heterocyclic systems with specific properties.
    In the field of materials science, it also has outstanding performance. It can participate in the preparation of special functional materials, such as some materials with excellent electrical conductivity, optical or adsorption properties. With its special interaction with other substances, it can adjust the microstructure and macroscopic properties of materials to meet different application requirements.
    Furthermore, in the field of biomedicine, 2-methyl-N-benzylimidazole may have potential biological activity. It can be used as a lead compound for researchers to further explore its pharmacological mechanism. After structural modification and optimization, it is expected to develop new drugs for the diagnosis and treatment of diseases. In chemistry and related fields, it is like a delicate brick and stone, laying the foundation for numerous research and applications, and promoting the continuous development of various fields.
    What are the physical properties of 2-Methyl-N-benzylimidazole?
    2-Methyl-N-benzylimidazole is one of the organic compounds. Its physical properties are particularly important, related to its many uses and characteristics.
    Predictive properties, this compound is mostly in a solid state at room temperature, with a certain crystallinity, or white to off-white powder, fine texture, this characteristic is quite critical in processing and identification.
    As for the melting point, it is about a specific temperature range. This temperature range is its inherent property and is extremely important for the determination of its purity and the temperature control of the processing process. If the melting point is consistent with the standard value, the purity is good; if it deviates, it may contain impurities.
    Solubility is also a key physical property. In common organic solvents, such as ethanol, acetone, etc., it exhibits a certain solubility, but its solubility in water is relatively limited. This property is an important basis for selecting suitable solvents during operations such as extraction, separation and preparation of solutions.
    In terms of density, it has a specific value. Although it is rarely directly involved in daily operations, it is an indispensable parameter in chemical production and the study of its distribution and behavior in mixed systems.
    In addition, its volatility is weak and it is not easy to evaporate and dissipate under normal conditions. This property guarantees its stability during storage and use without special volatilization protection measures.
    In addition, the color of 2-methyl-N-benzylimidazole is pure, almost colorless or microstrip light, and this color characteristic is essential in applications that require color, such as the preparation of some fine chemicals.
    From the above, the physical properties of 2-methyl-N-benzylimidazole play a crucial role in the application and research of chemical industry, materials, medicine and many other fields, and are the basis for its rational use, treatment and development of new uses.
    Is 2-Methyl-N-benzylimidazole chemically stable?
    The chemical stability of 2-methyl-N-benzyl imidazole depends on many factors. The structure of this substance is formed by the introduction of methyl and benzyl groups into the imidazole ring.
    Looking at its chemical activity, the methyl group has an electron-giving effect, which can affect the electron cloud density of the imidazole ring and then its reactivity. The presence of benzyl groups also plays a significant role in the spatial resistance and electronic properties of the molecule.
    Under normal conditions, 2-methyl-N-benzyl imidazole shows a certain stability. The aromatic structure of the imidazole ring itself gives it a certain chemical stability. However, under specific reaction conditions, such as strong oxidizing agents, strong acids, strong bases, etc., its stability will be challenged.
    If there is a strong oxidizing agent, the carbon and hydrogen bonds on the benzyl group may be oxidized, or the imidazole ring may be oxidized to open the ring. Strong acids and strong bases can also protonate or deprotonate with nitrogen atoms on the imidazole ring, thereby changing the electronic structure and reactivity of the molecule.
    In the field of organic synthesis, 2-methyl-N-benzyl imidazole is often used as a ligand or reaction intermediate. The characteristics of its stability not only ensure that it can exist stably in certain reaction steps and participate in specific reactions, but also because of moderate reactivity, it can be converted under suitable conditions to produce the desired product.
    In summary, the chemical stability of 2-methyl-N-benzylimidazole is not absolute, but varies depending on the environment and the chemical reagents encountered. Under mild conditions, it can remain relatively stable; but in extreme chemical environments, its stability will be shaken and corresponding chemical reactions will occur.
    What are 2-Methyl-N-benzylimidazole synthesis methods?
    The synthesis of 2-methyl-N-benzyl imidazole has been known for a long time, and there are many methods, and each has its own advantages.
    First, imidazole is used as the starting material, and under specific conditions, it undergoes a nucleophilic substitution reaction with benzyl halides. This process requires careful control of the reaction temperature, time and ratio of reactants. If the temperature is too high, side reactions will multiply; if the temperature is too low, the reaction rate will be slow. When the ratio of the two is appropriate, the target product can be effectively formed. If benzyl chloride reacts with imidazole, under the catalysis of alkali, stirring and refluxing in an organic solvent, after a few hours, after separation and purification, 2-methyl-N-benzyl imidazole can be obtained.
    Second, with 2-methylimidazole as the base, it can also be synthesized by synergistic action with aldehyde substances and reducing agents. First, 2-methylimidazole is condensed with benzaldehyde to generate the corresponding Schiff base, and then the Schiff base is reduced with a suitable reducing agent, such as sodium borohydride, etc., to obtain the target product. This approach requires attention to the mild reaction conditions to avoid excessive reduction or side reactions.
    Furthermore, the coupling reaction catalyzed by transition metals is also a feasible way. With suitable metal catalysts, such as palladium catalysts, the 2-methylimidazole derivative is coupled with benzyl halide or benzyl borate. This method requires strict reaction conditions, an oxygen-free environment, and the choice and dosage of catalysts are quite critical to the efficient synthesis of 2-methyl-N-benzyl imidazole.
    In the process of synthesis, the advantages and disadvantages of each method coexist. It is necessary to weigh the choices according to actual needs and operate carefully to obtain satisfactory results.
    What is the price of 2-Methyl-N-benzylimidazole in the market?
    2-Methyl-N-benzyl imidazole is found in the market, and its price varies from situation to situation, and it is difficult to determine a certain number. The price of this chemical substance is related to multiple ends, and the price of raw materials is the main reason. If the raw material is easy to harvest and abundant, the price may level; if it is thin and difficult to harvest, the price will rise. The preparation method is also heavy, and the process is expensive and laborious, and the price will be high; if it is simple and efficient, the price may be controllable. The market supply and demand situation, the price is very huge. There are many people in need but less supply, and the price will rise; if the supply exceeds the demand, the price will drop. In addition, the distance of the origin and the quality are all variables of the price. The place of origin is remote, and the cost of transportation is high, so the price goes up; the quality is high, and the self-worth is high. And the state of market competition also makes the price fluctuate. If the industry is competitive, or the price is given in order to occupy the market; if the oligarchs compete, the price will be stable or rising. Therefore, if you want to know the exact price, you should carefully observe the market conditions and compare the prices of others, so that you can get a more realistic number, and it is difficult to hide the geometry of the price.